This page contains affiliate links and Faith's Mom may earn a commission if you use them. As an Amazon Associate, Faith's Mom earns from qualifying purchases. Learn more. Ever since Faith was born, she has struggled with her digestion. When she was in the NICU, she would spit up after eating even the tiniest amount of formula. Her dad and I were convinced her tummy was too small to handle large volumes of food. Sometimes when she ate, her heart rate would drop really low, which is why she needed to be in the NICU for longer. She just could not get the hang of eating and breathing at the same time! Faith receiving food through an NG tube in the NICU. Grandma giving Faith a bottle when she was 2 months old. After finally bringing her home, eating continued to be an issue as she struggled with severe reflux and constipation. We tried various formulas, but she was never able to drink enough formula to gain a lot of weight. She also had trouble burping, and she...
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Faith's Integrative Music Sessions
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This past Sunday at church I noticed Faith singing along to the chorus with a little more gusto than she has in the past. She seemed a little more confident and really projected her voice once she caught on to the words that were being sung.
I must admit, listening to her sweet voice singing the words, "He is faithful, He is glorious, He is Jesus, all my hope is in Him. He is freedom, He is healing right now" was enough to cause tears to stream down my face. Later after thinking about it, I realized that part of her new-found confidence in singing probably has something to do with the integrative music sessions she has been doing with a music therapist.
Faith playing the xylophone
fun with shakers
Every couple of weeks, Jonnica comes into our home and spends about 30 minutes with Faith singing songs and playing instruments. I know how much Faith likes music so I was pretty sure she would enjoy doing this, but an added bonus is that the music therapist also does worship at her church so she and Faith like the same kind of music!
While Jonnica does fun songs with Faith like The Popcorn Song, Ravioli and The Shaker Song, they also sing songs like "This Little Light of Mine" and "He's Got the Whole World in His Hands."
The great part about this music therapy is that while it is super fun for Faith, it also helps her work on things like motor skills, cognition, communication, visual and auditory skills. Besides bringing instruments like shakers, bells and the xylophone for Faith to play, Jonnica also brings flashcards with letters, numbers, words and colors. One of Faith's favorite parts though is getting to play Jonnica's pretty red guitar.
working on more than just music
Of all the cool instruments, this is Faith's favorite!
We've only really begun the integrative music sessions this year, but I am already noticing differences in Faith and how it is helping her. I'm just as excited as Faith is about this type of therapy and who knows maybe she'll be helping to lead worship one day at church!
Click on the video below to hear Faith and Jonnica's good-bye song.
Dear Cari, Faith is just the most beautiful little girl. I have never heard exactly what she has for a handicap is it spina bifida or CP or something else? It is only important to me when I tell others about youtwo it is good to have the facts straight. I can't wait to meet her sometime! Hugs, Betty
Music therapy looks like so much fun! I am in favor of any type of education or therapy that really engages kids, gets them excited, and enriches their lives!
Guest Post by Stephen Gallup Last week, a columnist for the local newspaper interviewed me in connection with a memoir I wrote that’s being published this year. It was a comfortable, low-key discussion in which he asked about the basic facts regarding my disabled son Joseph and what I’ve learned that might be of value to other families. It was the sort of dialog that required no special preparation in advance. I just sat down with him and talked about the subject closest to my heart. But looking back on it now, one thing bothers me. In concluding the interview, the reporter expressed heartfelt sympathy for everything I’ve endured. He was being more than polite. I mean, he laid the compassion on with a spatula. Startled, and already thinking ahead to what I had to do next that day, I just thanked him and said goodbye. But now that final note troubles me. I don’t want sympathy! First of all, from the point of view of a new author hoping to promote his book, sympathy...
This page contains affiliate links and Faith's Mom may earn a commission if you use them. As an Amazon Associate, Faith's Mom earns from qualifying purchases. Learn more. Last year, when I heard the news that Pat Sajak was retiring from Wheel of Fortune , I knew I better prepare Faith. When season 41 began, I told her, "This is Pat's last season. Next year, there will be a new host." Faith likes Vanna but loves Pat! Faith and I have faithfully watched Wheel of Fortune every night since she was about 5 years old. It's how she learned that AEIOU were vowels. The show was also a great way to reinforce the rest of the alphabet. Counting was reinforced, too. When Vanna turned the letters, she counted how many T's, N's, or other letters there were. She also learned some geography skills with the different trips they gave away. Upon winning a trip to Aruba, she would ask, "Where's that?" Sometimes I honestly didn't know and had to loo...
This page contains affiliate links and Faith's Mom may earn a commission if you use them. As an Amazon Associate, Faith's Mom earns from qualifying purchases. Learn more. Ever since Faith was born, she has struggled with her digestion. When she was in the NICU, she would spit up after eating even the tiniest amount of formula. Her dad and I were convinced her tummy was too small to handle large volumes of food. Sometimes when she ate, her heart rate would drop really low, which is why she needed to be in the NICU for longer. She just could not get the hang of eating and breathing at the same time! Faith receiving food through an NG tube in the NICU. Grandma giving Faith a bottle when she was 2 months old. After finally bringing her home, eating continued to be an issue as she struggled with severe reflux and constipation. We tried various formulas, but she was never able to drink enough formula to gain a lot of weight. She also had trouble burping, and she...
Did you know there are 1 million people in the United States who have cerebral palsy? I guess that means Faith truly is one in a million! Faith was diagnosed with cerebral palsy when she was six months old. Prior to that, she had been given the diagnosis of Periventricular Leukomalacia (PVL). During her premature birth, there was a lack of oxygen to her brain, which resulted in damage to the white matter, or inner part of her brain. I will never forget receiving that news. Faith's Dad and I were told that nobody knew what the long-term effects of PVL would look like for her. All I could do was stare at my tiny daughter lying in her isolette, hooked up to all kinds of tubes and lines, and choose to believe she would be okay. Faith in the NICU a few days after she was born. After over 70 days in the NICU, we finally took her home to Watford City. There, she would receive regular visits from an Early Intervention team who would assess her and ensure that she met al...
Dear Cari,
ReplyDeleteFaith is just the most beautiful little girl. I have never heard exactly what she has for a handicap is it spina bifida or CP or something else? It is only important to me when I tell others about youtwo it is good to have the facts straight. I can't wait to meet her sometime!
Hugs,
Betty
Hi Betty, she was diagnosed with CP at 6 months of age. Blessings to you!
ReplyDeleteMusic therapy looks like so much fun! I am in favor of any type of education or therapy that really engages kids, gets them excited, and enriches their lives!
ReplyDelete